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Alzheimer disease in post-menopausal women: Intervene in the critical window period

Alzheimer disease (AD) is a crippling neurodegenerative disorder. It is more common in females after menopause. Estrogen probably has a protective role in cognitive decline. Large amount of research has been carried out to see the benefits of hormone replacement therapy with regards to Alzheimer sti...

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Detalles Bibliográficos
Autores principales: Jamshed, Nayer, Ozair, Fouzia Firdaus, Aggarwal, Praveen, Ekka, Meera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955045/
https://www.ncbi.nlm.nih.gov/pubmed/24672205
http://dx.doi.org/10.4103/0976-7800.127791
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author Jamshed, Nayer
Ozair, Fouzia Firdaus
Aggarwal, Praveen
Ekka, Meera
author_facet Jamshed, Nayer
Ozair, Fouzia Firdaus
Aggarwal, Praveen
Ekka, Meera
author_sort Jamshed, Nayer
collection PubMed
description Alzheimer disease (AD) is a crippling neurodegenerative disorder. It is more common in females after menopause. Estrogen probably has a protective role in cognitive decline. Large amount of research has been carried out to see the benefits of hormone replacement therapy with regards to Alzheimer still its neuroprotective effect is not established. Recent studies suggest a reduced risk of AD and improved cognitive functioning of post-menopausal women who used 17 β-estradiol in the critical period. Use of 17 β-estradiol in young and healthy post-menopausal women yields the maximum benefit when the neurons are intact or neuronal stress has just started. Hence intervention in the critical period is key in the prevention or delay of AD in post-menopausal women.
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spelling pubmed-39550452014-03-26 Alzheimer disease in post-menopausal women: Intervene in the critical window period Jamshed, Nayer Ozair, Fouzia Firdaus Aggarwal, Praveen Ekka, Meera J Midlife Health View Point Alzheimer disease (AD) is a crippling neurodegenerative disorder. It is more common in females after menopause. Estrogen probably has a protective role in cognitive decline. Large amount of research has been carried out to see the benefits of hormone replacement therapy with regards to Alzheimer still its neuroprotective effect is not established. Recent studies suggest a reduced risk of AD and improved cognitive functioning of post-menopausal women who used 17 β-estradiol in the critical period. Use of 17 β-estradiol in young and healthy post-menopausal women yields the maximum benefit when the neurons are intact or neuronal stress has just started. Hence intervention in the critical period is key in the prevention or delay of AD in post-menopausal women. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC3955045/ /pubmed/24672205 http://dx.doi.org/10.4103/0976-7800.127791 Text en Copyright: © Journal of Mid-life Health http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle View Point
Jamshed, Nayer
Ozair, Fouzia Firdaus
Aggarwal, Praveen
Ekka, Meera
Alzheimer disease in post-menopausal women: Intervene in the critical window period
title Alzheimer disease in post-menopausal women: Intervene in the critical window period
title_full Alzheimer disease in post-menopausal women: Intervene in the critical window period
title_fullStr Alzheimer disease in post-menopausal women: Intervene in the critical window period
title_full_unstemmed Alzheimer disease in post-menopausal women: Intervene in the critical window period
title_short Alzheimer disease in post-menopausal women: Intervene in the critical window period
title_sort alzheimer disease in post-menopausal women: intervene in the critical window period
topic View Point
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955045/
https://www.ncbi.nlm.nih.gov/pubmed/24672205
http://dx.doi.org/10.4103/0976-7800.127791
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